Reprocessed Non-Electric Biopsy Forceps Suppliers
EMAIL INQUIRY to 3 suppliers
Sterilmed, Inc. | Address: 11400 73rd Ave. North, #100, Maple Grove, Minnesota 55369, USA 
www.sterilmed.com | Send Inquiry | Phone: +1-(763)-488-3400, 888-252-1542
FDA Registration: 2134070
Products: Biopsy Forceps, Balloon Inflation Devices, Arthroscopy, Hook Probe, Burs & Drills, Burr, Arthroscopic Shavers, ...
Sterilmed, Inc. offers reprocessing, repair, and refurbishment of medical devices, equipment, and instruments. We also specialize in the sale of quality pre-owned surgical video equipment. Our pre-own more...
www.sterilmed.com | Send Inquiry | Phone: +1-(763)-488-3400, 888-252-1542
FDA Registration: 2134070
Products: Biopsy Forceps, Balloon Inflation Devices, Arthroscopy, Hook Probe, Burs & Drills, Burr, Arthroscopic Shavers, ...
Sterilmed, Inc. offers reprocessing, repair, and refurbishment of medical devices, equipment, and instruments. We also specialize in the sale of quality pre-owned surgical video equipment. Our pre-own more...
Medisiss | Address: 2747 Sw 6th Street, Redmond, Oregon 97756, USA
www.medisiss.com | Send Inquiry | Phone: +1-(541)-923-3310,866-866-7477
FDA Registration: 3032391
Products: Surgical Sterilizing Aids, Packaging, Instrument Cleaning System, Medical Devices, Instrument Maintenance & Refurbishing Service, Electrosurgical Cutting and Coagulation Device (FDA Code: GEI), ...
Medisiss is a registered third-party medical device reprocessor of single-use devices (SUDs).Our service list encompasses the cleaning, testing, refurbishing, sterilizing and packaging of both re-usab more...
www.medisiss.com | Send Inquiry | Phone: +1-(541)-923-3310,866-866-7477
FDA Registration: 3032391
Products: Surgical Sterilizing Aids, Packaging, Instrument Cleaning System, Medical Devices, Instrument Maintenance & Refurbishing Service, Electrosurgical Cutting and Coagulation Device (FDA Code: GEI), ...
Medisiss is a registered third-party medical device reprocessor of single-use devices (SUDs).Our service list encompasses the cleaning, testing, refurbishing, sterilizing and packaging of both re-usab more...
Stryker Trauma Gmbh | Address: Prof.-Kuentscher-Strasse 1-5, Schoenkirchen D-24232, Germany 
Phone: +49-(4348)-702-0
FDA Registration: 9610622 Year Established: 1941
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Flexible Depth Gauge (FDA Code: HTJ), Invasive Traction Component (FDA Code: JEC), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ), ...
Stryker Trauma GmbH offers orthopedic manual surgical instruments, pneumatic orthopedic power tool systems, screws and staples. more...
Phone: +49-(4348)-702-0
FDA Registration: 9610622 Year Established: 1941
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Flexible Depth Gauge (FDA Code: HTJ), Invasive Traction Component (FDA Code: JEC), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ), ...
Stryker Trauma GmbH offers orthopedic manual surgical instruments, pneumatic orthopedic power tool systems, screws and staples. more...
EMAIL INQUIRY to 3 Reprocessed Non-Electric Biopsy Forceps suppliers
FDA Code / Regulation: NON / 876.1075
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
Classification. (1) Class II (performance standards).
